A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477792



Internal ID22535693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21356526..21363917hg38UCSC Ensembl
chr18:18936487..18943878hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg387392
hg197392
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885322
Supporting Variants
Samples
Known GenesGREB1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477792
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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